Publications by authors named "Sergio Del Olmo-Cabrera"

Members of the synaptophysin and synaptogyrin family are vesicle proteins with four transmembrane domains. In spite of their abundance in synaptic vesicle (SV) membranes, their role remains elusive and only mild defects at the cellular and organismal level are observed in mice lacking one or more family members. Here, we show that coexpression with synapsin in fibroblasts of each of the four brain-enriched members of this family-synaptophysin, synaptoporin, synaptogyrin 1, and synaptogyrin 3-is sufficient to generate clusters of small vesicles in the same size range of SVs.

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Article Synopsis
  • - The Cre-Lox system is a popular method in biomedical research for making targeted gene deletions, allowing scientists to modify genes conditionally based on specific tissues or timeframes using Cre recombinase and LoxP sites.
  • - Existing methods to monitor Cre activity may not accurately reflect the deletion of other genes in the vicinity, leading to potential confusion in results.
  • - The new iSuRe-Cre mouse model enhances Cre activity in reporter-expressing cells, ensuring that researchers can trust the deletion of targeted genes, thereby improving the efficiency and reliability of studying gene functions.
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Unlabelled: Synaptophysins 1 and 2 and synaptogyrins 1 and 3 constitute a major family of synaptic vesicle membrane proteins. Unlike other widely expressed synaptic vesicle proteins such as vSNAREs and synaptotagmins, the primary function has not been resolved. Here, we report robust elevation in the probability of release of readily releasable vesicles with both high and low release probabilities at a variety of synapse types from knockout mice missing all four family members.

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Improved methods for manipulating and analyzing gene function have provided a better understanding of how genes work during organ development and disease. Inducible functional genetic mosaics can be extraordinarily useful in the study of biological systems; however, this experimental approach is still rarely used in vertebrates. This is mainly due to technical difficulties in the assembly of large DNA constructs carrying multiple genes and regulatory elements and their targeting to the genome.

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